Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the

7q31 deletion FOXP2 MLPA case report expressive speech disorder

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2021
Historique:
received: 05 02 2021
accepted: 22 07 2021
entrez: 7 9 2021
pubmed: 8 9 2021
medline: 8 9 2021
Statut: epublish

Résumé

Pathogenic variants of

Identifiants

pubmed: 34490154
doi: 10.3389/fped.2021.664548
pmc: PMC8417935
doi:

Types de publication

Case Reports

Langues

eng

Pagination

664548

Informations de copyright

Copyright © 2021 Nagy, Kárteszi, Elmont and Ujfalusi.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Orsolya Nagy (O)

Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Judit Kárteszi (J)

Hospital of Zala County, Zalaegerszeg, Hungary.

Beatrix Elmont (B)

Department of Pediatrics, Hospital of Zala County, Zalaegerszeg, Hungary.

Anikó Ujfalusi (A)

Division of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Classifications MeSH